Familial 22q11.2 Duplication/Deletion Syndrome: A Testament to the Long-Standing Clinical Utility of FISH.
Saved in:
| Title: | Familial 22q11.2 Duplication/Deletion Syndrome: A Testament to the Long-Standing Clinical Utility of FISH. |
|---|---|
| Authors: | Bryant LM; The Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA., Hokanson R; Department of Pediatrics, Section of Genetic and Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA., Hickey SE; Department of Pediatrics, Section of Genetic and Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.; Department of Pediatrics The Ohio State University Columbus Ohio USA., Zapanta B; Department of Pediatrics, Section of Genetic and Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA., Hunter J; The Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.; Department of Pediatrics The Ohio State University Columbus Ohio USA.; The Ohio State University Columbus Ohio USA., Reshmi SC; The Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.; Department of Pediatrics The Ohio State University Columbus Ohio USA.; The Ohio State University Columbus Ohio USA. |
| Source: | Clinical case reports [Clin Case Rep] 2025 Nov 14; Vol. 13 (11), pp. e71483. Date of Electronic Publication: 2025 Nov 14 (Print Publication: 2025). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: John Wiley & Sons Country of Publication: England NLM ID: 101620385 Publication Model: eCollection Cited Medium: Print ISSN: 2050-0904 (Print) Linking ISSN: 20500904 NLM ISO Abbreviation: Clin Case Rep Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 2050-0904 |
|---|---|
| DOI: | 10.1002/ccr3.71483 |
